vitelliform macular dystrophy
Information
- Disease name
- vitelliform macular dystrophy
- Disease ID
- DOID:0050661
- Description
- "A macular degeneration that it is characterized by the disruption of cells in a small area near the center of the retina, the macula and may cause progressive vision loss." [url:http\://en.wikipedia.org/wiki/Vitelliform_macular_dystrophy, url:http\://ghr.nlm.nih.gov/condition/vitelliform-macular-dystrophy]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
Genes | Mutation | Description | Source | Links |
---|
NCT ID | Status | Phase | Summary | Start date | Completion date |
---|---|---|---|---|---|
NCT04356716 | Active, not recruiting | Phase 2 | Sildenafil for Treatment of Choroidal Ischemia | November 11, 2014 | December 2024 |
- Exact Synonym (Disease Ontology)
- Best disease
- Exact Synonym (Disease Ontology)
- Best macular dystrophy
- Exact Synonym (Disease Ontology)
- juvenile-onset vitelliform macular dystrophy
- Disase is a (Disease Ontology)
- DOID:4448
- Cross Reference ID (Disease Ontology)
- GARD:10120
- Cross Reference ID (Disease Ontology)
- GARD:182
- Cross Reference ID (Disease Ontology)
- ICD10CM:H35.5
- Cross Reference ID (Disease Ontology)
- MESH:D057826
- Cross Reference ID (Disease Ontology)
- MIM:153700
- Cross Reference ID (Disease Ontology)
- MIM:153840
- Cross Reference ID (Disease Ontology)
- MIM:608161
- Cross Reference ID (Disease Ontology)
- MIM:616151
- Cross Reference ID (Disease Ontology)
- MIM:616152
- Cross Reference ID (Disease Ontology)
- ORDO:1243
- Cross Reference ID (Disease Ontology)
- ORDO:99000
- MeSH unique ID (MeSH (Medical Subject Headings))
- D057826